ClinVar Genomic variation as it relates to human health
GRCh37/hg19 Xq22.1-22.2(chrX:102543473-103398234)x0
Germline
Classification
(1)
Uncertain significance
no assertion criteria provided
Somatic
No data submitted for somatic clinical impact
Somatic
No data submitted for oncogenicity
Genes
Gene | OMIM | ClinGen Gene Dosage Sensitivity Curation | Variation Viewer | Related variants | ||
---|---|---|---|---|---|---|
HI score | TS score | Within gene | All | |||
PLP1 | Sufficient evidence for dosage pathogenicity | Sufficient evidence for dosage pathogenicity |
GRCh38 GRCh37 |
15 | 527 | |
BEX2 | - | - |
GRCh38 GRCh37 |
18 | 179 | |
BEX3 | - | - |
GRCh38 GRCh37 |
1 | 168 | |
H2BW1 | - | - |
GRCh38 GRCh37 |
27 | 203 | |
H2BW2 | - | - | - |
GRCh38 GRCh37 |
23 | 194 |
MORF4L2 | - | - |
GRCh38 GRCh37 |
5 | 181 | |
RAB40A | - | - |
GRCh38 GRCh37 |
- | 190 | |
RAB9B | - | - |
GRCh38 GRCh37 |
2 | 513 | |
SLC25A53 | - | - |
GRCh38 GRCh37 |
16 | 196 | |
TCEAL1 | - | - |
GRCh38 GRCh37 |
21 | 199 |
There are 7 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh37) and ClinGen Dosage Sensitivity Map.
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
- | RCV000993779.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022